Actively Recruiting

Age: 18Years +
All Genders
NCT07007598

Prevention of Post-Polypectomy Colorectal Bleeding by Clips in Patients on Anticoagulants

Led by Helios Kliniken Schwerin · Updated on 2025-06-18

10000

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

Sponsors

H

Helios Kliniken Schwerin

Lead Sponsor

M

Medical School Hamburg

Collaborating Sponsor

AI-Summary

What this Trial Is About

This observational study aims to retrospectively determine if clips can prevent post-polypectomy bleeding in adults who have received restarted anticoagulants after a colorectal polypectomy, using a large, single-center patient registry. The main question it aims to answer is: Can clips prevent post-polypectomy bleeding in adults who have received restarted anticoagulants after a colorectal polypectomy? Researchers will compare adults who received preventive clipping after a polypectomy with those who did not, regarding colorectal bleeding after receiving restarted anticoagulants. Participants have undergone a colorectal polypectomy and received restarted anticoagulants (acetylsalicylic acid excluded) after the procedure.

CONDITIONS

Official Title

Prevention of Post-Polypectomy Colorectal Bleeding by Clips in Patients on Anticoagulants

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult who has received a colonoscopy with endoscopic colorectal polypectomy
  • Patient who has received at least one anticoagulant after polypectomy
Not Eligible

You will not qualify if you...

  • Endoscopic polypectomy was combined with closure of the mucosal defect by a suturing device or full thickness resection device

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Helios Kliniken Schwerin

Schwerin, Mecklenburg-Vorpommern, Germany, 19055

Actively Recruiting

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Research Team

D

Daniel Schmitz, Dr. med.

CONTACT

M

Martin Kliment

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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